Shrimpton AE - Search Results

1

Development and characterization of reference materials for MTHFR, SERPINA1, RET, BRCA1, and BRCA2 genetic testing.

Barker SD, Bale S, Booker J, Buller A, Das S, Friedman K, Godwin AK, Grody WW, Highsmith E, Kant JA, Lyon E, Mao R, Monaghan KG, Payne DA, Pratt VM, Schrijver I, Shrimpton AE, Spector E, Telatar M, Toji L, Weck K, Zehnbauer B, Kalman LV. Barker SD, et al. Among authors: shrimpton ae. J Mol Diagn. 2009 Nov;11(6):553-61. doi: 10.2353/jmoldx.2009.090078. Epub 2009 Sep 18. J Mol Diagn. 2009. PMID: 19767587 Free PMC article.

2

Bioelectronic sensor technology for detection of cystic fibrosis and hereditary hemochromatosis mutations.

Bernacki SH, Farkas DH, Shi W, Chan V, Liu Y, Beck JC, Bailey KS, Pratt VM, Monaghan KG, Matteson KJ, Schaefer FV, Friez M, Shrimpton AE, Stenzel TT. Bernacki SH, et al. Among authors: shrimpton ae. Arch Pathol Lab Med. 2003 Dec;127(12):1565-72. doi: 10.5858/2003-127-1565-BSTFDO. Arch Pathol Lab Med. 2003. PMID: 14632577 Free article.

3

Genetically characterized positive control cell lines derived from residual clinical blood samples.

Bernacki SH, Beck JC, Stankovic AK, Williams LO, Amos J, Snow-Bailey K, Farkas DH, Friez MJ, Hantash FM, Matteson KJ, Monaghan KG, Muralidharan K, Pratt VM, Prior TW, Richie KL, Levin BC, Rohlfs EM, Schaefer FV, Shrimpton AE, Spector EB, Stolle CA, Strom CM, Thibodeau SN, Cole EC, Goodman BK, Stenzel TT. Bernacki SH, et al. Among authors: shrimpton ae. Clin Chem. 2005 Nov;51(11):2013-24. doi: 10.1373/clinchem.2005.048694. Epub 2005 Sep 15. Clin Chem. 2005. PMID: 16166172

4

Characterization of publicly available lymphoblastoid cell lines for disease-associated mutations in 11 genes.

Bernacki SH, Beck JC, Muralidharan K, Schaefer FV, Shrimpton AE, Richie KL, Levin BC, Pont-Kingdon G, Stenzel TT. Bernacki SH, et al. Among authors: shrimpton ae. Clin Chem. 2005 Nov;51(11):2156-9. doi: 10.1373/clinchem.2005.048686. Clin Chem. 2005. PMID: 16244288 No abstract available.

5

Cystic fibrosis: S158N (605G --> A) is a rare genetic variant found in coupling with deltaF508.

Hicks K, Beadling W, Shrimpton AE. Hicks K, et al. Among authors: shrimpton ae. Genet Test. 2003 Spring;7(1):73-6. doi: 10.1089/109065703321560985. Genet Test. 2003. PMID: 12820707

6

Cystic fibrosis mutation frequencies in upstate New York.

Shrimpton AE, Borowitz D, Swender P. Shrimpton AE, et al. Hum Mutat. 1997;10(6):436-42. doi: 10.1002/(SICI)1098-1004(1997)10:6<436::AID-HUMU4>3.0.CO;2-B. Hum Mutat. 1997. PMID: 9401006

7

Molecular diagnosis of cystic fibrosis.

Shrimpton AE. Shrimpton AE. Expert Rev Mol Diagn. 2002 May;2(3):240-56. doi: 10.1586/14737159.2.3.240. Expert Rev Mol Diagn. 2002. PMID: 12050863 Review.

8

R117H and IVS8-5T cystic fibrosis mutation detection by restriction enzyme digestion.

Shrimpton AE. Shrimpton AE. Mol Diagn. 2000 Sep;5(3):235-8. doi: 10.1054/modi.2000.9730. Mol Diagn. 2000. PMID: 11070158

9

Primary nodal marginal zone B-cell lymphoma arising from more than one clonal neoplastic population.

Finch CN, Nichols M, Shrimpton A, Liu D, Hutchison RE. Finch CN, et al. Arch Pathol Lab Med. 2000 Dec;124(12):1816-9. doi: 10.5858/2000-124-1816-PNMZBC. Arch Pathol Lab Med. 2000. PMID: 11100064 Free article.

10

Prenatal diagnosis for the cystic fibrosis mutation 1717-1, G-->A using arms.

Miedzybrodzka ZH, Kelly KF, Davidson M, Little S, Shrimpton AE, Dean JC, Haites NE. Miedzybrodzka ZH, et al. Among authors: shrimpton ae. Prenat Diagn. 1992 Oct;12(10):845-9. doi: 10.1002/pd.1970121012. Prenat Diagn. 1992. PMID: 1475255

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